Fromes Y, Gounon P, Tapiero H, Fellous A
Institut de Génétique Moléculaire, Laboratorie de Pharmacologie Expérimentale 27, Paris, France.
J Protein Chem. 1996 Aug;15(6):561-73. doi: 10.1007/BF01908538.
Anthracyclines are among the most useful agents for the treatment of neoplastic disease, but their clinical use is limited by progressive cardiomyopathy. A few studies have suggested the role of microtubules for the understanding of this toxicity. By using kinetic and structural studies, we demonstrate the disorganizing action of fluoro-doxorubicin, a novel anthracycline, on the microtubule system. Microtubules have a rich and complex composition in relation to their numerous functions in cells. In the present study, we investigate the role of two major microtubule-associated protein (MAP) families, Tau and MAP2. Both MAP families are responsible for the properties of different classes of microtubules. We show the differential effect of fluoro-doxorubicin on these two classes of microtubules. Furthermore, we show that fluoro-doxorubicin is able to affect the capacity of purified tubulin to form normal microtubules. This study confirms that anthracyclines may interfer with the microtubule organization. We suggest that some classes of microtubules, with regard to their MAP composition, may be affected more specifically in cardiac myocytes.
蒽环类药物是治疗肿瘤疾病最有效的药物之一,但其临床应用因进行性心肌病而受到限制。一些研究表明微管在理解这种毒性方面的作用。通过动力学和结构研究,我们证明了新型蒽环类药物氟柔比星对微管系统的破坏作用。微管因其在细胞中的众多功能而具有丰富而复杂的组成。在本研究中,我们研究了两个主要的微管相关蛋白(MAP)家族,即Tau和MAP2的作用。这两个MAP家族负责不同类别的微管的特性。我们展示了氟柔比星对这两类微管的不同作用。此外,我们表明氟柔比星能够影响纯化微管蛋白形成正常微管的能力。这项研究证实蒽环类药物可能干扰微管组织。我们认为,就其MAP组成而言,某些类别的微管可能在心肌细胞中受到更具体的影响。